Taiwan FDA registration de939a29855db9dd5eab897ddd608966
“Natus” Pre-Gelled Disposable Surface Electrode
TW: “納特斯”拋棄式表面電極
Taiwan·Risk Class 2·MD·Natus Neurology Incorporated·Registered Sep 16, 2019 – Sep 16, 2024ExpiredRegistration details
- Analysis ID
- de939a29855db9dd5eab897ddd608966
- License Form
- Ministry of Health Medical Device Import No. 032846
- Customs Code
- DHA05603284601
Company information
- Manufacturer
- Natus Neurology Incorporated
- Manufacturer Country
- United States
- Authorized Representative
- SYNGROWTH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1320 skin electrode
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 16, 2019
- Expiry Date
- Sep 16, 2024
About this record
Access comprehensive regulatory information for “Natus” Pre-Gelled Disposable Surface Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de939a29855db9dd5eab897ddd608966 and manufactured by Natus Neurology Incorporated. The authorized representative in Taiwan is SYNGROWTH CO., LTD..
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